Source: HPO

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 5189
Gene Symbol: PEX1
PEX1
CUI: C0002452
Disease: Amelogenesis Imperfecta
Amelogenesis Imperfecta 		0.400 Biomarker HPO

Entrez Id: 5189
Gene Symbol: PEX1
PEX1
CUI: C0018784
Disease: Sensorineural Hearing Loss (disorder)
Sensorineural Hearing Loss (disorder) 		0.110 Biomarker HPO

Entrez Id: 5189
Gene Symbol: PEX1
PEX1
CUI: C0035334
Disease: Retinitis Pigmentosa
Retinitis Pigmentosa 		0.110 Biomarker HPO

Entrez Id: 5189
Gene Symbol: PEX1
PEX1
CUI: C3714756
Disease: Intellectual Disability
Intellectual Disability 		0.110 Biomarker HPO

Entrez Id: 5189
Gene Symbol: PEX1
PEX1
CUI: C0000889
Disease: Acanthosis Nigricans
Acanthosis Nigricans 		0.100 Biomarker HPO

Entrez Id: 5189
Gene Symbol: PEX1
PEX1
CUI: C0001403
Disease: Addison Disease
Addison Disease 		0.100 Biomarker HPO

Entrez Id: 5189
Gene Symbol: PEX1
PEX1
CUI: C0001925
Disease: Albuminuria
Albuminuria 		0.100 Biomarker HPO

Entrez Id: 5189
Gene Symbol: PEX1
PEX1
CUI: C0003811
Disease: Cardiac Arrhythmia
Cardiac Arrhythmia 		0.100 Biomarker HPO

Entrez Id: 5189
Gene Symbol: PEX1
PEX1
CUI: C0004134
Disease: Ataxia
Ataxia 		0.100 Biomarker HPO

Entrez Id: 5189
Gene Symbol: PEX1
PEX1
CUI: C0005745
Disease: Blepharoptosis
Blepharoptosis 		0.100 Biomarker HPO

Entrez Id: 5189
Gene Symbol: PEX1
PEX1
CUI: C0006157
Disease: Breech Presentation
Breech Presentation 		0.100 Biomarker HPO

Entrez Id: 5189
Gene Symbol: PEX1
PEX1
CUI: C0009081
Disease: Congenital clubfoot
Congenital clubfoot 		0.100 Biomarker HPO

Entrez Id: 5189
Gene Symbol: PEX1
PEX1
CUI: C0010038
Disease: Corneal Opacity
Corneal Opacity 		0.100 Biomarker HPO

Entrez Id: 5189
Gene Symbol: PEX1
PEX1
CUI: C0010417
Disease: Cryptorchidism
Cryptorchidism 		0.100 Biomarker HPO

Entrez Id: 5189
Gene Symbol: PEX1
PEX1
CUI: C0011351
Disease: Dental Enamel Hypoplasia
Dental Enamel Hypoplasia 		0.100 Biomarker HPO

Entrez Id: 5189
Gene Symbol: PEX1
PEX1
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus 		0.100 Biomarker HPO

Entrez Id: 5189
Gene Symbol: PEX1
PEX1
CUI: C0013274
Disease: Patent ductus arteriosus
Patent ductus arteriosus 		0.100 Biomarker HPO

Entrez Id: 5189
Gene Symbol: PEX1
PEX1
CUI: C0013336
Disease: Dwarfism
Dwarfism 		0.100 Biomarker HPO

Entrez Id: 5189
Gene Symbol: PEX1
PEX1
CUI: C0015469
Disease: Facial paralysis
Facial paralysis 		0.100 Biomarker HPO

Entrez Id: 5189
Gene Symbol: PEX1
PEX1
CUI: C0015544
Disease: Failure to Thrive
Failure to Thrive 		0.100 Biomarker HPO

Entrez Id: 5189
Gene Symbol: PEX1
PEX1
CUI: C0017601
Disease: Glaucoma
Glaucoma 		0.100 Biomarker HPO

Entrez Id: 5189
Gene Symbol: PEX1
PEX1
CUI: C0018818
Disease: Ventricular Septal Defects
Ventricular Septal Defects 		0.100 Biomarker HPO

Entrez Id: 5189
Gene Symbol: PEX1
PEX1
CUI: C0019209
Disease: Hepatomegaly
Hepatomegaly 		0.100 Biomarker HPO

Entrez Id: 5189
Gene Symbol: PEX1
PEX1
CUI: C0020295
Disease: Hydronephrosis
Hydronephrosis 		0.100 Biomarker HPO

Entrez Id: 5189
Gene Symbol: PEX1
PEX1
CUI: C0020500
Disease: Hyperoxaluria
Hyperoxaluria 		0.100 Biomarker HPO